Colon Cancer: Gene >> TMPRSS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332149
Start	41467747:41467747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1454A>T
AA Mutation	p.Tyr485Phe(p.Y485F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332149
Start	41494490:41494490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104C>A
AA Mutation	p.Thr35Asn(p.T35N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332149
Start	41471953:41471953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928G>A
AA Mutation	p.Ala310Thr(p.A310T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332149
Start	41489582:41489582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>T
AA Mutation	p.Ala84Ser(p.A84S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000332149
Start	41480504:41480504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757262240
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Trp(p.R182W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332149
Start	41473438:41473438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375491952
CDS Mutation	c.786G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332149
Start	41466145:41466145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1476C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000332149
Start	41467745:41467745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456C>T
AA Mutation	p.Arg486Ter(p.R486*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332149
Start	41494518:41494519(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.75_76insA
AA Mutation	p.Tyr26IlefsTer57(p.Y26Ifs*57)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TMPRSS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332149
Start	41498125:41498125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9G>T
AA Mutation	p.Leu3Phe(p.L3F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript